AbbVie
Senior Manager Of Statistical Programming
The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Development Operations. Responsibilities include: Leading the statistical programming activities for one or more compounds/indications or a therapeutic area. Managing a team of statistical programmers and the resource planning for their assigned projects. Ensuring timely deliverables, that all quality processes are followed and consistency within the projects. Developing and overseeing the development of SAS programs for the creation of ADaM data sets following CDISC standards. Developing and overseeing the development of SAS programs for the creation of Tables, Listings and Figures. Ensuring consistency of ADaM data sets for individual studies and integrated data. Creating documentation for regulatory filings including reviewers guides and data definition documents. Leading the development of standard SAS Macros and the development of standard operating procedures. Managing, mentoring and creating career development plans for assigned staff. Participating in the recruitment and selection of new staff. Qualifications: This position will be required to sit on-site 3 days / week MS in Statistics, Computer Science or a related field with 9+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 11+ years of relevant experience. Minimum of 2 years experience leading a team of statistical programmers. In-depth understanding of SAS programming concepts and techniques related to drug development. In-depth understanding of CDISC Standards. In-depth understanding of the drug development process, including experience with regulatory filings. Ability to communicate clearly both oral and written. Ability to effectively represent the Statistical Programming Organization in cross functional teams. Ability to accurately estimate effort required for project related programming activities. Key Stakeholders: Directors of Statistics; Data Scientists; Medical Writers; Regulatory Publishers; Clinical Project Managers Additional Information: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. This job is eligible to participate in our long-term incentive programs AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
The Senior Manager of Statistical Programming is a leadership role which manages a team of statistical programmers in the research and development of new pharmaceutical products. The Senior Manager of Statistical Programming is responsible for leading the statistical programming activities for one or more compounds/indications or a therapeutic area. This role must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Development Operations. Responsibilities include: Leading the statistical programming activities for one or more compounds/indications or a therapeutic area. Managing a team of statistical programmers and the resource planning for their assigned projects. Ensuring timely deliverables, that all quality processes are followed and consistency within the projects. Developing and overseeing the development of SAS programs for the creation of ADaM data sets following CDISC standards. Developing and overseeing the development of SAS programs for the creation of Tables, Listings and Figures. Ensuring consistency of ADaM data sets for individual studies and integrated data. Creating documentation for regulatory filings including reviewers guides and data definition documents. Leading the development of standard SAS Macros and the development of standard operating procedures. Managing, mentoring and creating career development plans for assigned staff. Participating in the recruitment and selection of new staff. Qualifications: This position will be required to sit on-site 3 days / week MS in Statistics, Computer Science or a related field with 9+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 11+ years of relevant experience. Minimum of 2 years experience leading a team of statistical programmers. In-depth understanding of SAS programming concepts and techniques related to drug development. In-depth understanding of CDISC Standards. In-depth understanding of the drug development process, including experience with regulatory filings. Ability to communicate clearly both oral and written. Ability to effectively represent the Statistical Programming Organization in cross functional teams. Ability to accurately estimate effort required for project related programming activities. Key Stakeholders: Directors of Statistics; Data Scientists; Medical Writers; Regulatory Publishers; Clinical Project Managers Additional Information: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term incentive programs. This job is eligible to participate in our long-term incentive programs AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.